Canonical Allele Identifier: CA3873726

Gene: RAB23

Linked Data

• dbSNP Id: rs758628915
• ExAC: 6:57055258 C / T
• gnomAD v2: 6-57055258-C-T
• gnomAD v3: 6-57190460-C-T
• gnomAD v4: 6-57190460-C-T
• MyVariant Identifiers: chr6:g.57055258C>T (hg19) ; chr6:g.57190460C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.57190460C>T , CM000668.2:g.57190460C>T	GRCh38
NC_000006.11:g.57055258C>T , CM000668.1:g.57055258C>T	GRCh37
NC_000006.10:g.57163217C>T	NCBI36
NG_012170.1:g.36821G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000468148.6:c.*1G>A MANE Select	ENSP00000417610.1:n.*1G>A
ENST00000317483.4:c.*1G>A	ENSP00000320413.3:n.*1G>A
ENST00000468148.5:c.*1G>A	ENSP00000417610.1:n.*1G>A
NM_001278666.1:c.*1G>A	NP_001265595.1:n.*1G>A
NM_001278667.1:c.*1G>A	NP_001265596.1:n.*1G>A
NM_001278668.1:c.*1G>A	NP_001265597.1:n.*1G>A
NM_016277.4:c.*1G>A	NP_057361.3:n.*1G>A
NM_183227.2:c.*1G>A	NP_899050.1:n.*1G>A
NR_103822.1:n.574G>A
NM_016277.5:c.*1G>A MANE Select	NP_057361.3:n.*1G>A
NM_001278666.2:c.*1G>A	NP_001265595.1:n.*1G>A
NM_001278667.2:c.*1G>A	NP_001265596.1:n.*1G>A
NM_001278668.2:c.*1G>A	NP_001265597.1:n.*1G>A
NM_183227.3:c.*1G>A	NP_899050.1:n.*1G>A
NR_103822.2:n.567G>A